Technical Field
[0001] The present invention relates to a lubricating oil for heat transfer devices (the
oil being hereinafter referred to as "a refrigerator oil") and, more specifically,
it relates to a refrigerator oil having a number of satisfactory and well-balanced
performances including lubricity, hydrolysis resistance, heat stability, refrigerant
miscibility, electric insulating ability and the like.
Background Art
[0002] Owing to the restriction of fluorocarbons for preventing ozone layer destruction,
efforts are being made to replace chlorine-containing fluorocarbon refrigerant such
as CFC-11, CFC-12, HCFC-22 or the like used in refrigerating and air conditioning
machines with chlorine-free fluorocarbon refrigerants such as HFC-32, HFC-125, HFC-134a
or the like. Since naphthenic oils or paraffinic oils that have been conventionally
used as refrigerator oils have not satisfactory refrigerant miscibility, which is
one of the requisite performances of a refrigerator oil, when a chlorine-free fluorocarbon
refrigerant is used, the researches have been executed to use ester oils instead of
naphthenic or parafinic oils. Such ester oil-containing refrigerator oils (referred
to as "ester refrigerator oil(s)" hereinafter) are disclosed, for example, in National
Publication No.
Hei 3-505602 (
JP-A 3-505602) of International Publication for Patent Application and Japanese Patent Kokai (Laid-Open)
Publication
No. 3-128992 (
JP-A 3-128992).
[0003] In addition to the refrigerant miscibility, the refrigerator oils are required to
have a number of performances including lubricity, hydrolysis resistance, heat stability,
electric insulating ability and the like. However, an ester refrigerator oil having
all the above-mentioned performances which are satisfactory and well-balanced has
not developed heretofore.
Disclosure of the Invention
[0004] The present invention has been accomplished to solve the above-mentioned technical
problems, namely, to develop an excellent ester refrigerator oil having all requisite
performances including refrigerant miscibility, lubricity, hydrolysis resistance,
heat stability, electric insulating ability. Accordingly, an object of the present
invention is to provide a refrigerator oil having all the above-mentioned performances
which are achieved in good balance.
[0005] As a results of the intensive researches conducted by the present inventors to attain
the above described object, it is found that an excellent refrigerator oil having
the above-mentioned various performances can be obtained by using a specific ester
oil as the base oil.
[0006] The refrigerator oil according to the present invention comprises an ester obtained
from:
pentaerythritol; and
a carboxylic acid mixture comprising n-pentanoic acid in an amount of 30 to 50% by
mass; n-heptanoic acid in an amount of 20 to 50 % by mass and 3,5,5- trimethylhexanoic
acid in an amount of 5 to 30 % by mass, of the total amount of the carboxylic acid
mixture.
[0007] In the refrigerator oil according to the present invention, the contents of n-pentanoic
acid, n-heptanoic acid and 3,5,5-trimethylhexanoic acid are preferably within ranges
of 30 to 45% by mass, 25 to 45% by mass and 10 to 30% by mass, respectively.
[0008] The refrigerator oil according to the present invention further preferably comprises
an epoxy compound and/or a phosphorus compound. The epoxy compound is preferably at
least one compound selected from a group consisting of phenylglycidyl ether epoxy
compounds, glycidyl ester epoxy compounds, alicyclic epoxy compounds and epoxidized
aliphatic acid monoesters, among which phenylglycidyl ether epoxy compounds and/or
glycidyl ester epoxy compounds are more preferable.
[0009] A fluid composition for refrigerators according to the present invention comprises
the above-described refrigerator oil according to the present invention and a chlorine-free
fluorocarbon.
Best Mode for Carrying out the Invention
[0010] The best modes for carrying out the present invention will be explained in detail
hereinafter.
[0011] The refrigerator oil according to the present invention comprises an ester (hereinafter
referred to as "specific ester") obtained from pentaerythritol and a carboxylic acid
mixture comprising n-pentanoic acid in an amount of 30 to 50% by mass; n-heptanoic
acid in an amount of 20 to 50 % by mass and 3,5,5-trimethylhexanoic acid in an amount
of 5 to 30 % by mass, of the total amount of the carboxylic acid mixture.
[0012] Taking into particular consideration the miscibility with the refrigerant, the content
of n-pentanoic acid in the carboxylic acid mixture is not less than 30% by mass, of
the total amount of the carboxylic acid mixture. On the other hand, taking into particular
consideration the hydrolysis resistance, the content of n-pentanoic acid in the carboxylic
acid mixture is not more than 50 % by mass, preferably not more than 45 % by mass,
more preferably not more than 40% by mass, and further more preferably not more than
35 % by mass, of the total amount of the carboxyl acid misture.
[0013] Further, taking into particular consideration the lubricity, the content of n-heptanoic
acid in the carboxylic acid mixture is not less than 20 % by mass, preferably not
less than 25 % by mass and more preferably not less than 30 % by mass, of the total
amount of the carboxyl acid mixture. On the other hand, taking into particular consideration
the hydrolysis resistance, the content of n-heptanoic acid in the carboxylic acid
mixture is not more than 50 % by mass, preferably not more than 45 % by mass, more
preferably not more than 40 % by mass and further more preferably not more than 35
% by mass, of the total amount of the carboxyl acid mixture.
[0014] Further, taking into particular consideration of the hydrolysis resistance, the content
of 3,5,5-trimethylhexanoic acid in the carboxylic acid mixture is not less than 5
% by mass, preferably not less than 10 % by mass and more preferably not less than
15 % by mass, of the total amount of the carboxyl acid mixutre. On the other hand,
taking into particular consideration the miscibility with the refrigerant and the
lubricity, the content of 3,5,5-trimethylhexanoic acid in the carboxylic acid mixture
is not more than 30 % by mass, of the total amount of the carboxyl acid mixture.
[0015] The specific ester according to the present invention may be a partial ester wherein
a part of hydroxyl groups of pentaerythritol remain un-esterified, whereas a complete
ester wherein all the hydroxyl groups of pentaerythritol are esterified is preferable.
Further the specific ester according to the present invention may be a mixture of
a partial ester and a complete ester.
[0016] There is no particular limit in respect to the content of the specific ester in the
refrigerator oil according to the present invention, but in order to attain all the
well-balanced requisite performances including refrigerant miscibility, lubricity,
hydrolysis resistance, heat stability, electric insulating ability and so on, the
content of the specific ester is preferably not less than 50 % by mass, more preferably
not less than 70 % by mass, further more preferably not less than 80 % by mass and
most preferably less than 90 % by mass, of the total amount of the refrigerator oil.
[0017] The refrigerator oil according to the present invention is an oil comprising the
above-described specific ester, whereas it may be used in combination with a hydrocarbon
oil such as mineral oils, olefin polymers, naphthalene compounds or alkylbenzenes;
or an oxygen-containing synthetic oil such as polyglycols, polyvinyl ethers, ketones,
polyphenyl ethers, silicone, polysiloxanes, perfluoro ethers or esters other than
the above-described specific esters. The preferable ones among the above-listed oxygen-containing
synthetic oils are polyglycols, polyvinyl ethers and ketones.
[0018] The refrigerator oil according to the present invention comprising the specific ester
and, if required, the hydrocarbon oil and/or the oxygen-containing synthetic oil is
principally used as a base oil. The refrigerator oil according to the present invention
can be suitably used in the form of a base oil without any additive or used in combination
with various kinds of additives according to necessity.
[0019] In order to further improve the wear resistance and load capacity, the refrigerator
oil according to the present invention may further comprise at least one phosphorus
compound selected from a group consisting of phosphoric esters, acidic phosphoric
esters, amine salts of acidic phosphoric esters, chlorinated phosphoric esters and
phosphorous esters. These phosphorus compounds are esters of phosphoric acid or phosphorous
acid and an alkanol or a polyether type alcohol; or are derivatives thereof.
[0020] Specifically, the phosphoric esters include, for example, tributyl phosphate, tripentyl
phosphate, trihexyl phosphate, triheptyl phosphate, trioctyl phosphate, trinonyl phosphate,
tridecyl phosphate, triundecyl phosphate, tridodecyl phosphate, tritridecyl phosphate,
tritetradecyl phosphate, tripentadecyl phosphate, trihexadecyl phosphate, triheptadecyl
phosphate, trioctadecyl phosphate, trioleyl phosphate, triphenyl phosphate, tricresyl
phosphate, trixylyl phosphate, cresyl diphenyl phosphate, xylyl diphenyl phosphate
and the like. The acidic phosphoric esters include, for example, monobutyl acid phosphate,
monopentyl acid phosphate, monohexyl acid phosphate, monoheptyl acid phosphate, monooctyl
acid phosphate, monononyl acid phosphate, monodecyl acid phosphate, monoundecyl acid
phosphate, monododecyl acid phosphate, monotridecyl acid phosphate, monotetradecyl
acid phosphate, monopentadecyl acid phosphate, monohexadecyl acid phosphate, monoheptadecyl
acid phosphate, monooctadecyl acid phosphate, monooleyl acid phosphate, dibutyl acid
phosphate, dipentyl acid phosphate, dihexyl acid phosphate, diheptyl acid phosphate,
dioctyl acid phosphate, dinonyl acid phosphate, didecyl acid phosphate, diundecyl
acid phosphate, didodecyl acid phosphate, ditridecyl acid phosphate, ditetradecyl
acid phosphate, dipentadecyl acid phosphate, dihexadecyl acid phosphate, diheptadecyl
acid phosphate, dioctadecyl acid phosphate, dioleyl acid phosphate and the like. The
amine salts of acidic phosphoric esters include, for example, salts of the above acidic
phosphoric esters and amines such as methylamine, ethylamine, propylamine, butylamine,
pentylamine, hexylamine, heptylamine, octylamine, dimethylamine, diethylamine, dipropylamine,
dibutylamine, dipentylamine, dihexylamine, diheptylamine, dioctylamine, trimethylamine,
triethylamine, tripropylamine, tributylamine, tripentylamine, trihexylamine, triheptylamine
and trioctylamine. The chlorinated phosphoric esters include, for example, tris dichloropropyl
phosphate, tris chloroethyl phosphate, tris chlorophenyl phosphate, polyoxyalkylene
bis [di(chloroalkyl)] phosphate and the like. The phosphorous esters include, for
example, dibutyl phosphite, dipentyl phosphite, dihexyl phosphite, diheptyl phosphite,
dioctyl phosphite, dinonyl phosphite, didecyl phosphite, diundecyl phosphite, didodecyl
phosphite, dioleyl phosphite, diphenyl phosphite, dicresyl phosphite, tributyl phosphite,
tripentyl phosphite, trihexyl phosphite, triheptyl phosphite, trioctyl phosphite,
trinonyl phosphite, tridecyl phosphite, triundecyl phosphite, tridodecyl phosphite,
trioleyl phosphite, triphenyl phosphite, tricresyl phosphite. The mixtures of the
above compounds can be used.
[0021] In a case where these phosphorus compounds are incorporated into the refrigerator
oil according to the present invention, the amount of the phosphorus compounds to
be incorporated is not particularly limited, whereas in general the content of the
incorporated phosphorus compounds is preferably within a range of 0.01 to 5.0 % by
mass and more preferably within a range of 0.02 to 3.0 % by mass, of the total amount
of the refrigerator oil (i.e., the total amount of the base oil and all incorporated
additives).
[0022] Further, in order to further improve the hydrolysis resistance, the refrigerator
oil according to the present invention may further comprise at least one epoxy compound
selected from a group consisting of:
- (1) phenylglycidyl ether epoxy compounds,
- (2) alkylglycidyl ether epoxy compounds,
- (3) glycidyl ester epoxy compounds,
- (4) allyl oxirane compounds,
- (5) alkyl oxirane compounds,
- (6) alicyclic epoxy compounds,
- (7) epoxidized fatty acid monoesters, and
- (8) epoxidized vegetable oils.
[0023] (1) Phenylglycidyl ether epoxy compounds can concretely exemplified by phenylglycidyl
ether or alkylphenylglycidyl ethers. The alkylphenylglycidyl ethers mentioned here
include, for example, those having 1 to 3 alkyl groups each having 1 to 13 carbon
atoms, among which those having one alkyl group with 4 to 10 carbon atoms, for example,
n- butylphenylglycidyl ether, i-butylphenylglycidyl ether, sec- butylphenylglycidyl
ether, tert-butylphenylglycidyl ether, pentylphenylglycidyl ether, hexylphenylglycidyl
ether, heptylphenylglycidyl ether, octylphenylglycidyl ether, nonylphenylglycidyl
ether, decylphenylglycidyl ether are preferable.
[0024] (2) Alkylglycidyl ether epoxy compounds can be concretely exemplified by decylglycidyl
ether, undecylglycidyl ether, dodecylglycidyl ether, tridecylglycidyl ether, tetradecylglycidyl
ether, 2- ethylhexylglycidyl ether, neopentylglycoldiglycidyl ether, trimethylolpropanetriglycidyl
ether, pentaerythritoltetraglycidyl ether, 1,6- hexanedioldiglycidyl ether, sorbitolpolyglycidyl
ether, polyalkyleneglycolmonoglycidyl ether, polyalkyleneglycoldiglycidyl ether.
[0025] (3) Glycidyl ester epoxy compounds can be concretely exemplified by phenylglycidyl
esters, alkylglycidyl esters, alkenylglycidyl esters and the like, the preferable
examples of which include glycidyl-2,2-dimethyloctanoate, glycidyl benzoate, glycidyl
acrylate, glycidyl methacrylate and the like.
[0026] (4) Allyl oxirane compounds can be concretely exemplified by 1,2-epoxy styrene, alkyl-1,2-epoxy
styrene.
[0027] (5) Alkyl oxirane compounds can be concretely exemplified by 1,2-epoxybutane, 1,2-epoxypentane,
1,2-epoxyhexane, 1,2-epoxyheptane, 1,2-epoxyoctane, 1,2-epoxynonane, 1,2-epoxydecane,
1,2-epoxyundecane, 1,2-epoxydodecane, 1,2-epoxytridecane, 1,2- epoxytetradecane, 1,2-epoxypentadecane,
1,2-epoxyhexadecane, 1,2-epoxyheptadecane, 1,2-epoxyoctadecane, 1,2-epoxynonadecane,
1,2-epoxyicosane.
[0028] (6) Alicyclic epoxy compounds can be concretely exemplified by 1,2-epoxycyclohexane,
1,2-epoxycyclopentane, 3,4-epoxycyclohexylmethyl-3,4-epoxycyclohexanecarboxylate,
bis(3,4-epoxycyclohexylmethyl)adipate, exo-2,3-epoxynorbornane, bis(3,4-epoxy-6-methylcyclohexylmethyl)adipate,
2-(7-oxabicyclo[4.1.0]hept-3-yl)-spiro(1,3-dioxane-5,3'-[7]oxabicyclo[4.1.0])heptane,
4-(1'-methylepoxyethyl)-1,2-epoxy-2-methylcyclohexane, 4-epoxyethyl-1,2-epoxycyclohexane.
[0029] (7) Epoxidized fatty acid monoesters can be concretely exemplified by the esters
of an epoxidized fatty acid having 12 to 20 carbon atoms and a phenol, an alkylphenol
or an alcohol having 1 to 8 carbon atoms. In particular, butyl, hexyl, benzyl, cyclohexyl,
methoxyethyl, octyl, phenyl and butylphenyl esters of epoxidized stearic acid are
preferably used.
[0030] (8) Epoxidized vegetable oil can be concretely exemplified by the epoxy compounds
of vegetable oils such as soybean oil, linseed oil, cotton seed oil.
[0031] The preferable ones among the above-listed epoxy compounds are phenylglycidyl ether
epoxy compounds, glycidyl ester epoxy compounds, alicyclic epoxy compounds and epoxidized
fatty acid monoesters, among which phenylglycidyl ether epoxy compounds and glycidyl
ester epoxy compounds are more preferable, and phenylglycidyl ether, butylphenylglycidyl
ether, alkylglycidyl ester or the mixture thereof is particularly preferable.
[0032] When incorporating these epoxy compounds into the refrigerator oil according to the
present invention, the amount of the epoxy compounds to be incorporated is not particularly
limited, whereas in general the content of the incorporated epoxy compounds is preferably
within a range of 0.1 to 5.0% by mass and more preferably within a range of 0.2 to
2.0% by mass, of the total amount of the refrigerator oil (i.e., the total amount
of the base oil and all incorporated additives).
[0033] The refrigerator oil according to the present invention may be used in combination
with the above described phosphorus compounds and epoxy compounds, but in some cases,
the combination use of these two kinds of compounds is not preferable due to the possibility
of causing the generation of sludge.
[0034] Further, in order to improve the performances, the refrigerator oil according to
the present invention may be incorporated, as required, with heretofore known additives
for a refrigerator oil, for example, phenol-type antioxidants such as di-tert-butyl-p-cresol
and bisphenol A; amine-type antioxidants such as phenyl-α-naphthylamine and N,N-di(2-naphthyl)-p-phenylenediamine;
wear inhibitors such as zinc dithiophosphate; extreme pressure agents such as chlorinated
paraffin and sulfur compounds; oiliness improvers such as fatty acids; antifoaming
agents such as silicone-type ones; metal inactivators such as benzotriazole; viscosity
index improvers; pour-point depressants; detergent dispersants and so on. These additives
may be incorporated into the refrigerator oil singly or jointly. The total amount
of the additives added into the refrigerator oil is not particularly limited, whereas
in general the content thereof is preferably not more than 10% by mass and more preferably
not more than 5% by mass, of the total amount of the refrigerator oil (i.e., the total
amount of the base oil and all incorporated additives).
[0035] The kinematic viscosity of the refrigerator oil of the present invention is not particularly
limited, whereas the kinematic viscosity at 40°C can preferably be within a range
of 3 to 100 mm
2/s, more preferably 4 to 50 mm
2/s and the most preferably 5 to 40 mm
2/s. Further, the kinematic viscosity at 100°C can preferably be within a range of
1 to 20 mm
2/s and more preferably 2 to 10 mm
2/s.
[0036] Further, the volume resistivity of the refrigerator oil according to the present
invention is not particularly limited, whereas it can preferably be not less than
1.0×10
12Ω·cm, more preferably not less than 1.0×10
13Ω·cm and the most preferably not less than 1.0×10
14Ω·cm. Particularly, in a case when the refrigerator oil is used for a closed type
refrigerator, high electric insulating ability tends to become requisite. In the present
invention, the volume resistivity is represented by the value at 25°C measured in
accordance with JIS C 2101.
[0037] The refrigerator oil according to the present invention is particularly useful when
a chlorine-free fluorocarbon is used as the refrigerant. The chlorine-free fluorocarbon
may be a hydrofluorocarbon (HFC) having 1 to 3 carbon atoms and preferably 1 to 2
carbon atoms, for example, difluoromethane (HFC-32), trifluoromethane (HFC-23), pentafluoroethane
(HFC-125), 1,1,2,2-tetrafluoroethane (HFC-134), 1,1,1,2-tetrafluoroethane (HFC-134a),
1,1,1-trifluoroethane (HFC-143a), 1,1- difluoroethane (HFC-152a) or a mixture of two
or more kinds of these HFCs.
[0038] The refrigerant is selected in accordance with the use and the requisite performances.
For example, single HFC-32; single HFC-23; single HFC-134; single HFC-125, a mixture
of HFC-134a/HFC-32 = 60-80% by mass/40-20% by mass; a mixture of HFC-32/HFC-125 =
40-70% by mass/60-30% by mass; a mixture of HFC-125/HFC-143a = 40-60% by mass/60-40%
by mass; a mixture of HFC-134a/HFC-32/HFC-125 = 60% by mass/30% by mass/10% by mass;
a mixture of HFC-134a/HFC-32/HFC-125 = 40-70% by mass/15-35% by mass/5-40% by mass;
and a mixture of HFC-125/HFC-134a/HFC-143a = 35-55% by mass/1-15% by mass/40-60% by
mass are preferable. More specific examples include a mixture of HFC-134a/HFC-32 =
70/30% by mass, a mixture of HFC-32/HFC-125 = 60/40% by mass; a mixture of HFC-32/HFC-125
= 50/50% by mass (R410A); a mixture of HFC-32/HFC-125 = 45/55% by mass (R410B); a
mixture of HFC-125/HFC-143a = 50/50% by mass (R507C); a mixture of HFC-32/HFC-125/HFC-134a
= 30/10/60% by mass; a mixture of HFC-32/HFC-125/HFC-134a = 23/25/52% by mass (R407C);
a mixture of HFC-32/HFC-125/HFC-134a = 25/15/60% by mass (R407E); and a mixture of
HFC-125/HFC-134a/HFC-143a = 44/4/52% by mass (R404A).
[0039] The refrigerator oil of the present invention is also useful when a hydrocarbon is
used as the refrigerant. The hydrocarbon refrigerant is preferably a gas at 25°C under
1 atm, for example, alkane, cycloalkane or alkene having 1 to 5 carbon atoms and preferably
1 to 4 carbon atoms or a mixture thereof.
[0040] The examples of the hydrocarbon refrigerant include methane, ethylene, ethane, propylene,
propane, cyclopropane, butane, isobutane, cyclobutane, methylcyclopropane and the
mixtures of two or more kinds of these compounds, among which propane, butane, isobutane
and the mixtures thereof are preferable.
[0041] Further, the refrigerator oil according to the present invention is also useful when
a mixture of the chlorine-free fluorocarbon and the hydrocarbon refrigerant is used
as the refrigerant. The mixing ratio of the chlorine-free fluorocarbon and the hydrocarbon
is not particularly limited, but if a flame resistant refrigerant is pursued, the
ratio of HFC/hydrocarbon is preferably 50-97% by mass/50-3% by mass, more preferably
70-95% by mass/30-5% by mass and particularly preferably 80-90% by mass/20-10% by
mass. Further, the most preferable combination is HFC-32/propane, butane and/or isobutane
= 80-90% by mass/20-10% by mass if taking into consideration the flame resistance
and thermodynamic characteristic.
[0042] Furthermore, the refrigerator oil according to the present invention is also useful
when carbon dioxide is used as the refrigerant.
[0043] The refrigerator oil according to the present invention normally exists in the form
of a fluid composition for a refrigerator mixed with a refrigerant as describe above
when it is used in the refrigerator. The ratio of the refrigerator oil to the refrigerant
is not particularly limited, whereas the amount of the refrigerator oil is preferably
within a range of 1 to 500 parts by weight and more preferably within a range of 2
to 400 parts by weight per 100 parts by weight of the refrigerant.
[0044] The refrigerator oils according to the present invention may be used for lubricating
oils for refrigerant compressors in all types of refrigerators, since the present
refrigerator oils have an excellent electric characteristic and a low hygroscopicity.
Such refrigerators in which the present refrigerator oils are used can be concretely
exemplified by an air conditioner for rooms, a package air conditioner, a cold-storage
chest (refrigerator), an air conditioner for vehicles, a dehumidifier, a freezer,
a freeze and refrigeration warehouse, an automatic vending machine, a showcase, a
cooling apparatus in chemical plants and so on. Further, the refrigerator oil according
to the present invention is particularly preferable to be used in refrigerators having
a closed compressor. Furthermore, the refrigerator oil according to the present invention
can be used in all types of compressors including a reciprocating type one, a rotating
type one and a centrifugal type one.
[EXAMPLES]
[0045] The present invention will be explained in detail by the following Examples and Comparative
Examples, but the present invention is not limited to these Examples.
Example 1-3 and Comparative Example 1-3
[0046] The following base oils and additives were blended in the proportions shown in Table
1 to prepare sample oils of Examples 1-3 and Comparative Example 1-3, respectively.
The properties of each of the obtained sample oils are shown in Table 1 (kinematic
viscosities at 40°C and 100°C, total acid value and hydroxyl value).
- Base oil 1:
- tetraester of pentaerythritol and a carboxylic acid mixture consisting of n-pentanoic
acid (40% by mass), n-heptanoic acid (40% by mass) and 3,5,5-trimethylhexanoic acid
(20% by mass)
- Base oil 2:
- tetraester of pentaerythritol and n-pentanoic acid
- Base oil 3:
- tetraester of pentaerythritol and n-heptanoic acid
- Base oil 4:
- tetraester of pentaerythritol and 3,5,5-trimethylhexanoic acid
- Additive 1:
- glycidyl-2,2-dimethyloctanoate
- Additive 2:
- tricresyl phosphate
[0047] Next, the following tests were carried out in respect to each of the above-described
sample oils.
(Refrigerant Miscibility Test)
[0048] 5g of each of the sample oils was blended with 25g of the refrigerant (R407C) and
the upper critical temperature (the lowest temperature at which the refrigerant and
the sample oil dissolve mutually) was measured in accordance with "Refrigerant Miscibility
Testing Method" of JIS-K-2211 "Refrigerator oil." The results (upper critical temperature)
are shown in Table 1.
(Electric Insulating Ability Test)
[0049] The volume resistivity (at 25°C) of each of the sample oils was measured in accordance
with JIS-C-2101 "Electric Insulating Oil Testing Method." The results are shown in
Table 1.
(Heat Stability Test)
[0050] 90g of each of the sample oils, 30g of the refrigerant (R407C) and catalysts (iron,
copper and aluminum wires) were sealed in an autoclave and subsequently heated at
175°C. Two weeks later, the appearances of the sample oils, the appearance of the
catalysts, the volume resistivity of the sample oils and the total acid values of
the sample oils were measured. The results are shown in Table 1.
(Lubricity Test)
[0051] The sample oils were each applied to a test journal for measuring the amount of the
test journal (pin) worn by having the test machine run in at a test oil temperature
of 100°C under a load of 150 lb for 1 minute and then run under a load of 250 lb for
2 hours in accordance with ASTM D 2670 "FALEX WEAR TEST." The results of the measurement
are shown in Table 1.
(Hydrolysis Resistance Test)
[0052] 90g of each of the sample oils, 0.09 g of water and 30g of the refrigerant (R407C)
were introduced into a glass test tube having a volume of 300ml, then a copper wire,
a iron wire and an aluminum wire were placed therein as deterioration accelerating
catalysts. Subsequently, the tube was heated in an autoclave made of stainless steel
at 175°C for 168 hours to deteriorate the sample oil. The total acid value of each
sample oil after the test was measured and the results are shown in Table 1 together
with the total acid values before the test.
TABLE 1
|
Example 1 |
Example 2 |
Example 3 |
Comparative
Example 1 |
Comparative
Example 2 |
Comparative
Example 3 |
Base oil |
1 |
1 |
1 |
2 |
3 |
4 |
(% by mass) |
100 |
95.5 |
99 |
100 |
100 |
100 |
Additive |
- |
1 |
2 |
- |
- |
- |
(% by mass) |
|
0.5 |
1 |
|
|
|
Kinematic
viscosity |
40°C (mm2/s) |
28.5 |
28.5 |
28.5 |
15.8 |
21.6 |
115 |
100°C (mm2/s) |
5.50 |
5.50 |
5.50 |
3.67 |
4.50 |
11.5 |
Total acid value (mgKOH/g) |
0.01 |
0.01 |
0.01 |
0.01 |
0.01 |
0.01 |
Hydroxyl value (mgKOH/g) |
0.9 |
2.5 |
2.9 |
0.8 |
1.0 |
1.8 |
Upper critical temperature (°C) |
-35 |
-34 |
-33 |
<-50 |
-5 |
13 |
Volume resistivity (Ω·cm) |
8.7 × 1014 |
9.3 × 1014 |
4.9 × 1014 |
2.3 × 1014 |
4.8 × 1014 |
1.8 × 1014 |
Heat stability test |
Appearance of sample oil |
No change |
No change |
No change |
No change |
No change |
No change |
Appearance of catalyst |
No change |
No change |
No change |
Glossy
reduced |
Glossy reduced |
No change |
Volume resistivity (Ω·cm) |
5.4 × 1014 |
7.4 × 1014 |
2.0×1014 |
1.8×1014 |
3.6×1014 |
1.0×1014 |
Total acid value (mgKOH/g) |
0.02 |
0.01 |
0.01 |
0.03 |
0.03 |
0.02 |
FALEX test |
Amount of journal worn (mg) |
13 |
14 |
6 |
18 |
15 |
26 |
Hydrolysis resistance |
Total acid value (mgKOH/g) |
0.05 |
0.01 |
0.21 |
0.87 |
0.62 |
0.06 |
[0053] It is shown clearly by the results stated in Table 1 that the sample oils in Examples
1 to 3 of the refrigerator oil according to the present invention have the excellent
and well-balanced performances including not only the refrigerant miscibility with
the chlorine-free fluorocarbon refrigerants but also lubricity, hydrolysis resistance,
heat stability, electric insulating ability and kinematic viscosity.
[0054] On the contrary, the sample oil of Comparative Example 1 which used tetraester of
pentaerythritol and n-pentanoic acid was inferior in lubricity and hydrolysis resistance.
Further, the sample oil of Comparative Example 2 which used tetraester of pentaerythritol
and n-heptanoic acid was inferior in refrigerant miscibility and hydrolysis resistance.
Furthermore, the sample oil of Comparative Example 3 which used tetraester of pentaerythritol
and 3,5,5-trimethylhexanoic acid was inferior in refrigerant miscibility and lubricity.
Industrial Applicability
[0055] As described above, according to the refrigerator oil of the present invention, the
excellent and well-balanced requisite performances including not only the refrigerant
miscibility with the chlorine-free fluorocarbon refrigerants but also lubricity, hydrolysis
resistance, heat stability, electric insulating ability and the like can be attained.